During development, cells signal to one another to communicate positional information that directs them to take on appropriate fates and form contacts with the correct partners. We study these processes using the visual system of the fruit fly Drosophila as our primary model. The repetitive yet exquisitely organized structure of the Drosophila eye and the power of unbiased genetic screens have enabled us to uncover general mechanisms by which cells communicate.
We have identified novel components of the Hedgehog, Wnt, Notch, and epidermal growth factor (EGF) receptor pathways that are important for patterning the fly eye and are misregulated in cancer and other human diseases.
We also study how cell–cell signals are translated into cell fate decisions through effects on specific transcriptional or post-transcriptional regulators of gene expression. Visual system assembly requires neurons to identify and form synapses with the correct partners, in order to form a functional neural circuit. We are investigating the molecular basis for synaptic partner selection, as well as the mechanisms that allow synapse size to grow in proportion to the size of the target.
For further details on my research, please visit the Treisman Lab website .
Professor, Department of Cell Biology
Coord Developmental Genetics Prog
PhD from Rockefeller University
Journal of cell science. 2018 Sep 20; 131(18):
The Drosophila Epidermal Growth Factor Receptor does not act in the nucleus
Journal of cell science. 2018 Sep 01; 131(18):
Development. 2018 Feb 05; 145(3):
PLoS genetics. 2018 Jan 11; 14(1):e1007173-e1007173
Development. 2017 Jun 15; 144(14):2673-2682
Development. 2015 Apr 15; 142(8):1480-1491
Genes & development. 2014 Aug 15; 28(16):1786-1799